PRO-Pharmaceuticals,inc.

CLINICAL TRIAL SECURED SERVER

Data Menu

CRF Completion Guidelines	Import Data from Medidata	Development of PK Log per MP request
Data Management Plan	Export Data	Teleconferences
Date Edit Specification	Data Management staff and Maintenance	Document Management – Trial Master File
Data Base Creation	Design Analysis Plan	Document Management - CRF
Consistency Check Creation	Program Derived Datasets & Populations	Document Management - Initial Approval
CRF Tracking	Program Tables Figures and Listings	Document Management - Maintenance
CRF Data Entry & Verification	Statistical Analysis	Document Management - Annual IRB Approval
CRF Review	Pre-Results-Clinical Study Report	Financial Disclosure
Administer Local Labs	Bullet Summary – Clinical Study Report	Clinical Trial Agreements
Process Queries	Clinical Scientist Maintenance	Clinical Trial Storage and Distribution
Coding	Medical Writer Staff Maintenance	SAE Reporting - Regulatory Agencies world
QC Review of Data	Revise Investigation Brochures	IND Safety Report